2'-Fluoro-4'-methoxyacetophenone → 2-(2-Fluoro-4-methoxyphenyl)-2-propanol

HRID 1994515Notes

Reaction equation

HRID 1994515 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10](=[O:12])[CH3:11].[CH3:13][Mg+].[Br-]>C1COCC1>[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10]([OH:12])([CH3:13])[CH3:11]

Participants

4

Conditions

Temperature
0 °C

Procedure

To a solution of 2′-fluoro-4′-methoxyacetophenone (4.45 g, 26.5 mmol) in THF (50 ml) at 0° C., a solution of 2.4 M MeMgBr (11.6 mmol, 27.8 mmol) was added. The mixture was stirred at 0° C. and then room temperature for 4 h. The reaction was quenched with saturated ammonium chloride solution. The organic was extracted with ethyl acetate (3×50 ml). The combined ethyl acetate layers were washed with brine and dried over sodium sulfate. The resulting alcohol was obtained as an oil after flash column using EtOAc:hexane=2:8 as the elute.

Workup

  1. customThe reaction was quenched with saturated ammonium chloride solution
  2. extractionThe organic was extracted with ethyl acetate (3×50 ml)
  3. washThe combined ethyl acetate layers were washed with brine
  4. dry with materialdried over sodium sulfate

Sources & evidence

ORD record
ord-041938c1139a48d0a0e96a03ce0b1a34
Source dataset
uspto-grants-2010_01
Patent number
US07652049B2

Reaction notes

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